Early-onset familial hemiplegic migraine due to a novel SCN1A mutation

INTRODUCTION: Familial hemiplegic migraine (FHM) is a rare autosomal dominant subtype of migraine with aura. The FHM3 subtype is caused by mutations in SCN1A, which is also the most frequent epilepsy gene encoding the voltage-gated Na(+) channel Na(V)1.1. The aim of this study was to explore the cli...

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Publicat a:Cephalalgia
Autors principals: Fan, Chunxiang, Wolking, Stefan, Lehmann-Horn, Frank, Hedrich, Ulrike BS, Freilinger, Tobias, Lerche, Holger, Borck, Guntram, Kubisch, Christian, Jurkat-Rott, Karin
Format: Artigo
Idioma:Inglês
Publicat: SAGE Publications 2016
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Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5105328/
https://ncbi.nlm.nih.gov/pubmed/26763045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0333102415608360
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